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Clinical and Diagnostic Laboratory Immunology, April 2005, p. 542-547, Vol. 12, No. 4
1071-412X/05/$08.00+0     doi:10.1128/CDLI.12.4.542-547.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Rapid Competitive Enzyme-Linked Immunosorbent Assay for Detection of Antibodies to Peste des Petits Ruminants Virus

Kang-Seuk Choi,1* Jin-Ju Nah,1 Young-Joon Ko,1 Shien-Young Kang,2 and Nam-In Jo1

Foreign Animal Disease Division, National Veterinary Research and Quarantine Service, Anyang, Kyoung-gi,1 Research Institute of Veterinary Medicine/College of Veterinary Medicine, Chungbuk National University, Heungduk-Ku, Cheongju, Chungbuk, Korea2

Received 13 September 2004/ Returned for modification 6 December 2004/ Accepted 14 January 2005

Peste des petits ruminants (PPR) is a contagious viral disease of small ruminants that is of economic importance in Africa, the Middle East, and Asia. We developed a rapid competitive enzyme-linked immunosorbent assay (rapid c-ELISA) for the diagnosis and surveillance of PPR. This assay detects PPR virus (PPRV) antibodies in serum samples by quantifying the amount of monoclonal antibody (MAb) P-3H12 after 30 min of incubation of a serum-MAb conjugate mixture on plates coated with a PPRV recombinant nucleocapsid protein (rPPRV-N). We tested 249 PPRV-positive serum samples and 733 PPRV-negative serum samples from field ruminants. The threshold of percent inhibition (PI) was determined to be <50 on the basis of the mean PI plus 3 standard deviations for sera from PPRV-negative ruminants. The relative specificity and sensitivity of the rapid c-ELISA were 98.5% (722 of 733 serum samples) and 93.4% (234 of 249 serum samples), respectively. The rapid c-ELISA sensitively detected PPRV antibodies in hyperimmune sera (virus neutralization test [VNT] titer, >512), even at dilutions ≥512 in normal goat serum, and as early as 6 to 13 days postinfection from 12 goats, each of which was infected with one of the four PPRV lineages. Hyperimmune sera from animals experimentally vaccinated with rinderpest virus gave positive results by the rapid c-ELISA when the rinderpest virus VNT titers were >512, although the rapid c-ELISA titers were very low (2 to 16). However, the rapid c-ELISA was negative when the rinderpest virus VNT titer was ≤128. The rapid c-ELISA developed in the present work provides a short turnaround time and could be a useful tool for the diagnosis of PPR and screening for PPRV in the field.

* Corresponding author. Mailing address: Foreign Animal Disease Division, National Veterinary Research and Quarantine Service, 480 Anyang-6 dong, Anyang, Kyoung-gi, 430-824, Korea. Phone: 82-31-467-1860. Fax: 82-31-449-5882. E-mail: choiks{at}nvrqs.go.kr.

Clinical and Diagnostic Laboratory Immunology, April 2005, p. 542-547, Vol. 12, No. 4
1071-412X/05/$08.00+0     doi:10.1128/CDLI.12.4.542-547.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.





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